- 2
- 1
Stephane Roche
3
Documents
Publications
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 3
- 3
- 3
- 3
- 3
- 3
- 3
- 2
- 2
- 2
- 2
- 2
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 1
- 3
- 1
- 2
- 1
- 1
- 1
|
SMCHD1 is involved in de novo methylation of theDUX4-encoding D4Z4 macrosatelliteiScience, 2022, 25 (2), pp.103757. ⟨10.1093/nar/gkz005⟩
Article dans une revue
hal-02002680v1
|
|
Deciphering the complexity of the 4q and 10q subtelomeres by molecular combing in healthy individuals and patients with facioscapulohumeral dystrophyJournal of Medical Genetics, In press, ⟨10.1136/jmedgenet-2018-105949⟩
Article dans une revue
hal-02140159v1
|
|
Methylation hotspots evidenced by deep sequencing in patients with facioscapulohumeral dystrophy and mosaicismNeurology Genetics, 2019, 5 (6), pp.e372. ⟨10.1212/NXG.0000000000000372⟩
Article dans une revue
hal-02406985v1
|